CRA
Clinical Careers Page(1 month ago)
About this role
A Clinical Research Associate II based in Chengdu within ICON plc’s Study Start Up team. The mid-level role is part of a global healthcare intelligence and clinical research organization and supports clinical development programs and trials.
Required Skills
- Site Monitoring
- Protocol Compliance
- Data Review
- Patient Safety
- Clinical Documentation
- ICH-GCP
- Communication
- Organization
- Stakeholder Collaboration
- Travel
Qualifications
- Bachelor's Degree
- Valid Driver's License
About Clinical Careers Page
iconplc.comICON plc is a global clinical research organisation (CRO) that provides outsourced clinical development and commercialisation services to pharmaceutical, biotechnology and medical device companies. It offers end-to-end drug and device development support — including clinical trial management across phases, data management and biostatistics, regulatory and safety/pharmacovigilance, and commercialisation and market-access services. ICON combines scientific and therapeutic expertise with technology and a scalable global operations network to accelerate development and bring therapies to patients. Clients engage ICON for integrated, experienced CRO support across the full product lifecycle.
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